Society Logo
Millie
Meet Millie, the Only Kangaroo in the Whole ME/CFS Universe!


Facebook


E-mail
Email the Society
Donations
Donations


ME/CFS AUSTRALIA (SA) INC

Registered Charity 698

Mailing address:
GPO Box 383,
Adelaide,
South Australia 5001

Office:
266 Port Road,
Hindmarsh,
South Australia 5007
Ph: (08) 8346 3237
('834 MECFS')

Office Hours:
Wednesdays, 10am-3pm

Support Line:
(Mondays and Thursdays,
10am-3pm)
Ph: (08) 8346 3237

SA country callers:
Ph: 1300 128 339
(local call)


FIBROMYALGIA HELP:
Contact
Fibromyalgia SA
at the
Arthritis Foundation of SA
118 Richmond Road,
Marleston 5033
Ph: (08) 8379 5711



ME/CFS Australia (SA) Inc supports the needs of sufferers of Myalgic Encephalomyelitis, Chronic Fatigue Syndrome and related illnesses. We do this by providing services and information to members.



Charity Direct

ME/CFS Australia (SA) Inc is a member of Charity Direct.



ourcommunity.com.auDonate online

Information and Support 2004 is an online appeal that aims to improve our Information and Support Line.

Read more…



Disclaimer

ME/CFS Australia (SA) Inc aims to keep members informed of the various research projects, diets, medications, therapies etc. All communication, both verbal and written, is merely to disseminate information and not to make recommendations or directives.

Unless otherwise stated, the views expressed on this Web site are not necessarily the official views of the Society or its Committee and are not simply an endorsement of products or services.

Print

Printer-friendly version


Vice-President’s Report
March 2001

1: Introduction
2: Who’s going to...?
3: Why a high turnover?
4: Independent teams
5: Issues to address
6: The way forward?
7: Conclusion


Reports
President’s report (AGM Nov 8, 2003)
Management Committee report (Jan 2003)
President’s end of year reports (2002)
President’s report (Mar 2002)
President’s report (Jan 2002)
President’s report (Nov 2001)
Nat. Assn. President’s report (Nov 2001)
President’s report (Sep 2001)
Miscellaneous reports (Jun 2001)
Vice-president’s report (Jun 2001)
Vice-president’s report (Mar 2001)

Vice-President’s Report

March 2001

(With illness hitting our President, Boris Dontscheff, I’ve undertaken to write this report)

By Paul Leverenz

Introduction

I’m sure you will agree that ME/CFS is a dreadful illness. It’s chronic, it’s invisible, and it’s poorly understood. We certainly have a lot of things that appear to conspire against us at times.

I’ll give you a classic example of how tough it is. A person with ME/CFS recently went to court to dispute his rejected Centrelink application for the Disability Support Pension. He decided to represent himself on the advice of legal counsel. His appeal was rejected – one of the reasons given was that he represented himself so well. By doing a good job they thought he couldn’t possibly be sick enough to warrant the pension.

Ironic, isn’t it? We all know we can gear ourselves up to perform for a short period of time, but it is not indicative of how we are the other 6.5 days of the week. Yes, we face an uphill battle to increase understanding, don’t we?

Next: Who’s going to look out for us? Next
Previous Previous Page